Muralidhar joined Watsi on September 23rd, 2016. Five years ago, Muralidhar joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Muralidhar's most recent donation supported Jecinta, a humorous tween from Kenya, to fund corrective surgery for her legs to boost her self-confidence.
Muralidhar has funded healthcare for 65 patients in 11 countries.
Muralidhar has funded healthcare for 65 patients in 11 countries.
Meet Jecinta, a 12-year-old friendly, talkative, and funny girl. She is the youngest in her family of three children. Currently, Jecinta is a student in grade 5, and in school, she likes reading and playing with her friends even though her legs limits her ability to play as well as her peers. Jecinta's mother is a single mother who works temporary jobs on neighbor’s farms, clothes washing, and other available jobs. Jecinta was born healthy, but her mother noticed a sudden bowing of her legs when she was one. Jecinta's mother took her toddler to a nearby hospital where plaster was applied to her legs to prevent spreading of her condition. However, since then, it has continued to worsen and has been affecting Jecinta's mobility. At this point, she cannot stand upright and play with friends as she would like to. Fortunately, Jecinta is scheduled to undergo surgery on July 19th to correct her legs. This treatment will allow her to walk like other friends, play with them, and continue with her studies, all of which can improve her self-esteem. “I would wish for support for my child because I cannot be able to afford the hospital bills,”Jecinta’s mother asks.
Ku is a seven-year-old boy who lives with his parents and two younger sisters in a refugee camp in Northern Thailand. Ku's mother weaves shirts that she sells, and Ku's father helps weave, too. Ku is a primary school student, while one of his sisters is in nursing school, and his youngest sister is too young to go to school. On June 6th, Ku and two of his friends were playing in a tamarind tree when they all fell out of the tree. Ku injured his left arm in the fall and his father carried him to the camp hospital for an exam. The medic there told Ku's father that his elbow might be broken. After they bandaged his arm, Ku visited another hospital for an x-ray and was diagnosed with a left elbow fracture. Ku is in pain and cannot bend his arm or lift anything. With the help of our medical partner, Burma Children Medical Fund (BCMF), Ku will undergo surgery to reset his fractured bones and ensure proper healing. The procedure is scheduled for June 9th and will cost $1,500. After surgery, Ku will no longer be in pain and he will be able to go back to school. He will regain full mobility in his arm. Ku's father shared, "Ku is an active boy who loves school and reading a lot. He always says that he wants to become a health worker to look after his family and others when he grows up. I want him to recover and go back to school soon."
Savorn is a 21-year-old construction worker from Cambodia. He lives with his parents and two siblings. In his free time, Savorn likes to listen to music on his phone and watch Khmer boxing on TV. In August 2020, Savorn was in a motor vehicle accident which caused a fracture of his left femur. After the accident, he went to a local Khmer healer, but his leg did not heal. As a result of the accident, Savorn cannot work or walk without assistance and he says that he feels poorly and is depressed. It is difficult for him to walk, and he is in chronic pain. Fortunately, surgeons at our medical partner, Children's Surgical Centre (CSC), can help Savorn. Savorn is currently in traction to align his fracture. On March 2nd, Savorn will undergo a fracture repair procedure, which will cost $465. This procedure will stabilize his fracture for permanent healing and will help him walk again. Savorn hopes after surgery, his left femur will be fixed, he will have no pain, and that can return to work to support his family.
Zawadi is a one month old infant from Tanzania. Her name means "gift" in Swahili, because to her parents she is a gift from God. Her parents are small scale farmers who mainly grow food crops like maize and vegetable for their own use at home. The father also seeks day jobs at construction sites to be able to supplement their living, and through the money they get from this work, they are able to pay bills and buy other home commodities. Zawadi has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of her condition, Zawadi has been experiencing an increasing head circumference. Without treatment, Zawadi will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $765 to cover the cost of surgery for Zawadi that will treat her hydrocephalus. The procedure will drain the excess fluid from Zawadi's brain, to reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Zawadi will hopefully develop into a strong, healthy young girl. Zawadi’s mother says "It’s been a step at a time trying to treat my daughter, but money is what has been our biggest challenge. She needs another surgery. Please help my daughter."
Shoh is a 47-year-old man who lives with his wife, two sons, daughter-in-law and two daughters in Nu Poe Refugee Camp in Thailand. In the camp, Shoh and his oldest son are teachers who teach about the Quran for other refugees. They each earn 1,200 baht (approx. 40 USD) per month. His wife is often sick, and his eldest daughter has to look after her at home. His daughter-in-law is a homemaker while his youngest daughter and son are students. Shoh’s household receives 1,110 baht (approx. 37 USD) every month on a cash card to purchase rations in the camp. Their monthly household income is just enough to cover their daily expenses as they also receive free basic health care and education in the camp. Since February 2020, Shoh has had umbilical hearnia. Currently, Shoh’s abdomen pain is not severe but his hernia is still increasing in size. He feels uncomfortable when he walks because of his swollen abdomen. He cannot sleep well and is increasingly worried about his diagnosis. The pain in his abdomen increases when he feels cold, especially at night. Fortunately, on March 9th, he will undergo hernia repair surgery at Mae Sot General Hospital, our medical partner's care center. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund Shoh's hernia repair surgery. The procedure is scheduled to take place on March 9th and, once completed, will hopefully allow him to live more comfortably. Shoh said, “I do not want to stop being a teacher. I love teaching the Quran to young children. Also, if I do not teach, I do not earn an income and my family does not have enough income to cover our household expenses.”
Daw Mya is a 59-year-old woman from Burma. She lives with her daughter, granddaughter, son, daughter-in-law, and grandson in Yangon, Burma. Daw Mya is currently too ill to work, but her daughter works as a seamstress in a factory. Her granddaughter goes to school, her son is a taxi driver, her daughter-in-law looks after their son at home. Her daughter and her son both help look after Daw Mya and try to support her as best they can. Daw Mya was diagnosed with a heart condition that involves a malformation of the mitral valve, the valve between the left atrium and left ventricle. This valve controls the flow of blood, but certain conditions may cause blood to flow backward or the valve to narrow. Currently, Daw Mya feels tired and experiences heart palpitations with chest pain. She has no appetite and cannot sleep well at night, and both of her legs are swollen. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a mitral valve replacement for Daw Mya. The treatment is scheduled to take place on February 21st and, once completed, will hopefully allow her to live more comfortably. Daw Mya said, “I want to get better soon so that I can help my family. I want to help them because my daughter-in-law is always looking after me and her child [my grandson], so she cannot work. If I can look after the household chores and take care of the family, they can go to work and earn more income for our family. I cannot go anywhere because of my condition. They always take care of me and they spend too much of their money on me.”
Jue is a 25-year-old woman who lives with her family in a village in Hmawbi Township, Yangon Division, Burma. Her parents are housekeepers, and her youngest brother is a first-year university student who has been seeking work. Jue used to run a beauty salon, but had to stop working four months ago when her health deteriorated. In her free time, Jue likes to watch the news and videos relating to her work at the beauty salon. She also likes to read books and wants to write a book of her own someday. In August 2020, Jue felt pains in her stomach and chest. She would also experience difficulty breathing sometimes, and she would feel tired when she walked for a longer period of time. Jue went to the clinic in her village, where she received oral medication, but she did not feel better after taking it. She returned to the clinic several times over the course of two months, but her condition continued to worsen – the chest pain, difficulty breathing and feeling of fatigue happened more often. Jue decided to go to another clinic in North Okkala Township in Yangon in November 2020. At the clinic, the doctor listened to her heart with a stethoscope, and informed her that she has a congenital heart condition. The doctor recommended she receive a blood test, an echocardiogram (echo) and an electrocardiogram (ecg) at a hospital. After visiting a hospital to receive those tests, the doctor there told her that she was born with a hole in her heart and that she might need to receive surgery at the general hospital. However, the cost of surgery was too high. Luckily, Jue crossed paths with another former patient and was referred to Watsi's Medical Partner Burma Children Medical Fund (BCMF) to seek assistance with accessing treatment. Fortunately, surgeons at our medical partner can help. On January 24th, U Win will undergo an atrial septal defect closure procedure. Once recovered, her quality of life will significantly improve and she will be able to return to working at her beauty salon. Now, our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund this procedure. Jue shared, “I want to get better as quickly as possible and go back to work. I’m worried about my younger brother. He doesn’t have a job, and he needs to graduate from university. I’m also worried about Covid-19 because nobody has a job right now.”
Khaing is a 27-year-old woman from Thailand. She lives with her husband and a three-year-old son in a village in Tak Province. Originally from Karen State, Burma, they moved to their current home three years ago in search of better job opportunities. Her husband is a day laborer and she is homemaker. Ten years ago, Khaing started feeling like her nose was blocked and that she could not breathe well. She also had a runny nose and saw a small mass in her nostril while looking at her reflection in the mirror. At the time, Khaing did not go to see a doctor because she could not afford to pay for treatment, and she thought that she would feel better over time. However, four years ago she noticed that the mass had grown. Khaing went to her local hospital in Burma, where the doctor confirmed she had a mass in her nostril and gave her medication for a week. She did not go back to her follow-up appointment as she had run out of money. She then tried to treat herself with traditional medicine unsuccessfully as the mass continued to increase in size. In the beginning of May 2020, Khaing developed a severe headache and pain in her nose. The area around her nose also became swollen. She went to Mae Tao Clinic for treatment, where the medic found large masses in both of her nasal cavities. She was then taken to Mae Sot Hospital (MSH) for further investigation. At MSH, she received an x-ray of her nose and the doctor told her that the masses were large and surrounded by a lot of pus. After a CT scan, the doctor diagnosed her with a nasal polyp and scheduled her for surgery on December 28th, 2020. Currently, the area around her nose is swollen and painful. Her nostrils feel itchy, her nose is blocked, and has to breathe through her mouth. She still has a headache, though since she received pain medication from the doctor at MSH, this has been less severe. Fortunately, surgeons at our medical partner can help. On December 28th, Khaing will undergo an endoscopic sinus surgery. Once recovered, she will be able to breathe normally again and her quality of life will significantly improve. Now, our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund this procedure. Khaing shared, "I really want to have surgery and feel better. I am not scared because I believe that the surgery will help me be free from headaches and breathe well again."
Beatrice is a young student from Kenya. She is a calm girl and the seventh born in a family of eight children. Her family hails from Mokoyon village in West Pokot County. Beatrice's father is a farmer while her mother is a housewife. They live in a one roomed grass thatched house in their village. Beatrice has clubfoot of her right foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Beatrice traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on November 23th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Beatrice's clubfoot repair. After treatment, she will be able to walk easily, play, and wear shoes like the other children she knows. “We are requesting for support so that her foot can be corrected and she can continue with her normal life,” Julius, Beatrice’s father told us.
Sandar is is a 48-year-old pastor from Burma. She lives with her husband, daughter, and seven children who she is sheltering. In her free time, Sandar likes to prepare for her sermons, read the Bible, and pray for others in need. Since 2017, Sandar has been experiencing high blood pressure and heavy abnormal vaginal bleeding. She has been diagnosed with pelvic mass and has been advised to undergo a total abdominal hysterectomy, the surgical removal of her uterus and cervix. If left untreated, Sandar's symptoms will continue to worsen and put her at risk for further health complications in the future. Fortunately, Sandar is scheduled to undergo her hysterectomy on February 24th. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to cover the total cost of her procedure and care. Once recovered, she will no longer experience abnormal bleeding or discomfort. "I worry about the children I shelter," said Sandar. "Currently, I have to buy a lot of sanitary pads and my daughter borrowed 500,000 kyat (approx. 500 USD) from her boss to support me, which she will pay back in installments.”
Srey Srors is a 19-year-old rice farmer from Cambodia. She has one older brother, and in her spare time she enjoys watching television and helping around the house with the cooking and cleaning. In June 2019, Srey Sors was in a severe motorcycle accident that resulted in damaging nerve injuries to her upper left arm. She has been diagnosed with a brachial plexus injury on her left side. The brachial plexus is a nerve network that transmits signals from the spine to the shoulder, arm, and hand. Injuries to this nerve network can result in loss of function and sensation. She is unable to move her left arm and cannot return to her work on the rice farm. Srey Srors traveled to our medical partner's care center to receive treatment. On December 10th, she will undergo a brachial plexus repair surgery. After recovery, she will be able to use her arm again. Our medical partner, Children's Surgical Centre, is requesting $637 to fund this procedure. "I hope that after my surgery, can use my arm again and return to my work at the rice fields," shared Srey Srors.
Megan is a 3-month old baby girl from Tanzania, and the only child to her single mother. Megan was born with clubfoot and spina bifida, which contributed to her acquiring hydrocephalus. Megan’s father left their family when her mother was five months pregnant and they lost any contact with him. Megan's grandmother, who was also a single mom after her husband passed away at a young age, depends on selling second-hand clothes. Her income is very limited to be able to provide for her children and be able to afford school fees. Due to this, Megan's mother was not able to continue with her studies due to financial challenges and joined her mother in selling second hand clothes. Megan has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of her condition, Megan has been experiencing an increasing head circumference. Without treatment, Megan will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,300 to cover the cost of surgery for Megan that will treat her hydrocephalus. The procedure is scheduled to take place on September 21st and will drain the excess fluid from Megan's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Megan will hopefully develop into a strong, healthy young girl. Megan’s mother says, “I have no one to run to for help and support, all my relatives have told me they can no longer support us in any way and yet my daughter is suffering. Please help save my daughter.”